Application of Human Brain Organoids-Opportunities and Challenges in Modeling Human Brain Development and Neurodevelopmental Diseases

被引:20
|
作者
Kim, Soo-hyun [1 ,2 ]
Chang, Mi-Yoon [1 ,2 ,3 ,4 ]
机构
[1] Grad Sch Biomed Sci & Engn, Dept Biomed Sci, Seoul 04763, South Korea
[2] Hanyang Univ, Biomed Res Inst, Seoul 04763, South Korea
[3] Hanyang Univ, Coll Med, Dept Premed, Seoul 04763, South Korea
[4] Hanyang Univ, Hanyang Inst Biosci & Biotechnol, Seoul 04763, South Korea
关键词
brain organoid; neurological disease; disease modeling; cell therapy; neural stem cell; HUMAN CORTICAL ORGANOIDS; STEM-CELL THERAPY; CEREBRAL ORGANOIDS; SELF-ORGANIZATION; MATURATION; MICE; GENERATION; MICROGLIA; FEATURES; DEFICITS;
D O I
10.3390/ijms241512528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain organoids are three-dimensional (3D) structures derived from human pluripotent stem cells (hPSCs) that reflect early brain organization. These organoids contain different cell types, including neurons and glia, similar to those found in the human brain. Human brain organoids provide unique opportunities to model features of human brain development that are not well-reflected in animal models. Compared with traditional cell cultures and animal models, brain organoids offer a more accurate representation of human brain development and function, rendering them suitable models for neurodevelopmental diseases. In particular, brain organoids derived from patients' cells have enabled researchers to study diseases at different stages and gain a better understanding of disease mechanisms. Multi-brain regional assembloids allow for the investigation of interactions between distinct brain regions while achieving a higher level of consistency in molecular and functional characterization. Although organoids possess promising features, their usefulness is limited by several unresolved constraints, including cellular stress, hypoxia, necrosis, a lack of high-fidelity cell types, limited maturation, and circuit formation. In this review, we discuss studies to overcome the natural limitations of brain organoids, emphasizing the importance of combinations of all neural cell types, such as glia (astrocyte, oligodendrocytes, and microglia) and vascular cells. Additionally, considering the similarity of organoids to the developing brain, regionally patterned brain organoid-derived neural stem cells (NSCs) could serve as a scalable source for cell replacement therapy. We highlight the potential application of brain organoid-derived cells in disease cell therapy within this field.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Modeling human neurodevelopmental diseases with brain organoids
    Xiaoxiang Lu
    Jiajie Yang
    Yangfei Xiang
    Cell Regeneration, 11
  • [2] Modeling human neurodevelopmental diseases with brain organoids
    Lu, Xiaoxiang
    Yang, Jiajie
    Xiang, Yangfei
    CELL REGENERATION, 2022, 11 (01)
  • [3] Modeling brain development and diseases with human cerebral organoids
    Shi, Yingchao
    Wu, Qian
    Wang, Xiaoqun
    CURRENT OPINION IN NEUROBIOLOGY, 2021, 66 : 103 - 115
  • [4] Brain Organoids as Tools for Modeling Human Neurodevelopmental Disorders
    Adams, Jason W.
    Cugola, Fernanda R.
    Muotri, Alysson R.
    PHYSIOLOGY, 2019, 34 (05) : 365 - 375
  • [5] Modeling Neurological Diseases With Human Brain Organoids
    Wang, Hansen
    FRONTIERS IN SYNAPTIC NEUROSCIENCE, 2018, 10
  • [6] Human brain organoids: development and application
    Xiang, Yangfei
    CANCER SCIENCE, 2022, 113 : 806 - 806
  • [7] Brain Organoids: Studying Human Brain Development and Diseases in a Dish
    Xu, Jie
    Wen, Zhexing
    STEM CELLS INTERNATIONAL, 2021, 2021
  • [8] Modeling human brain development with cerebral organoids
    Luca Muzio
    G Giacomo Consalez
    Stem Cell Research & Therapy, 4
  • [9] Modeling human brain development with cerebral organoids
    Muzio, Luca
    Consalez, G. Giacomo
    STEM CELL RESEARCH & THERAPY, 2013, 4
  • [10] Modeling Somatic Mutations Associated With Neurodevelopmental Disorders in Human Brain Organoids
    Deb, Bipan K.
    Bateup, Helen S.
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2022, 14